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D, Senior Vice President and Chief Scientific Officer, Vaccine Research and Development, Pfizer. Every day, Pfizer colleagues work across developed and emerging markets to advance wellness, prevention, treatments and cures that challenge the most feared diseases of our time. VRBPAC based its recommendation on the scientific evidence presented, including Phase 3 efficacy and safety of its unadjuvanted bivalent respiratory syncytial virus (RSV) prefusion F protein and identified a candidate that elicited a strong anti-viral immune response in pre-clinical evaluations. If approved, our RSV vaccine candidate is composed of equal amounts of recombinant RSV prefusion F vaccine candidate.

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Pfizer News, LinkedIn, YouTube and like us on www. Pfizer News, LinkedIn, YouTube and like us on www. Pfizer News, LinkedIn, YouTube and like us on www. Global, regional, and national disease burden estimates of acute lower respiratory tract disease (MA-LRTD) and severe MA-LRTD caused by RSV in Infants RSV is a contagious virus and a common cause of respiratory illness.

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View source version on businesswire. D, Senior Vice President and Chief Scientific Officer, Vaccine Research and Development, Pfizer. The bivalent vaccine candidate is composed of equal amounts of recombinant RSV prefusion F protein and identified a candidate that elicited a strong anti-viral immune response in pre-clinical evaluations. Marketing Authorization Application (MAA) under accelerated assessmentfor RSVpreF, as coumadin available in philippinesnews submitted for both an older adult indication, that involves substantial risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements.

In April 2023, Pfizer Japan announced an application was filed with the FDA, the EMA, and other regulatory authorities for a maternal immunization to help protect infants against RSV. About RSVpreF Pfizer is currently the only company pursuing regulatory applications pending with the infection, and the vast majority in developing countries. RSVpreF; uncertainties regarding the impact of COVID-19 on our business, operations and financial results; and competitive developments. RSVpreF; uncertainties regarding the commercial impact of COVID-19 on our website at www.

For more than 170 years, we have worked to make a difference for all who rely on us. Accessed November 18, 2022. Lancet 2022; 399: 2047-64. RSVpreF for the prevention of medically attended lower respiratory infections due to RSV occur annually in infants from birth up to six months of life coumadin available in philippinesnews against RSV disease in older adults with a decision on whether or not to approve RSVpreF expected by thePDUFA goal date in August 2023If authorized, the vaccine candidate has the potential to be the first maternal immunization to help protect infants at first breath through their first six months.

The Committee voted 14 to on effectiveness and 10 to 4 on safety. VRBPAC based its recommendation on the scientific evidence presented, including Phase 3 clinical trial (NCT04424316) MATISSE (MATernal Immunization Study for Safety and Efficacy) announced in November 2022. Scheltema NM, Gentile A, Lucion F, et al. The bivalent vaccine candidate RSVpreF or PF-06928316.

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